CASCADE recovers promoter-associated regulatory motifs from cell-type-resolved DNA language-model attributions
Gene expression is governed by regulatory DNA and their associated trans factors acting in specific cell types, yet the sequences underlying this control remain poorly mapped in plants. Genome-pretrained DNA language models provide a route to interrogate regulatory sequence directly, but their attributions have largely been interpreted using bulk or whole-tissue data, and standard attribution pipelines can preferentially highlight sequences downstream of the transcription start (TSS) site rather than promoter-associated signals. Here, we train a celltype-resolved sequence-to-expression model from a single-cell soybean (Glycine max) atlas by coupling a soybean-adapted Genomic Pre-trained Network (GPN) to a shared sequence encoder with 66 cell-type-specific output heads. Across 38,339 protein-coding genes, the model achieves a mean per-cell-type, across-gene Pearson correlation of 0.683 and, recast as a highversus-low expression classification, reaches an area under the ROC curve of 0.92 to 0.97 across tissues, at or above dedicated plant sequence models. We then introduce ContextAware Significance of Cross-gene Attribution for Discovering Elements (CASCADE), a positionspecific statistical framework for identifying model-derived candidate regulatory elements from in silico saturation mutagenesis. Relative to the pooled null used by TF-MoDISco, CASCADE shifts motif recovery from downstream of the transcription start site toward promoter sequence, with 77% of CASCADE-exclusive motifs, compared with 12% of TF-MoDISco-exclusive motifs, falling within the promoter. Applied across the atlas, CASCADE identifies approximately 1.39 million candidate elements spanning broadly active, tissue-restricted and cell-type-restricted classes. Together, these analyses establish a position-aware approach for extracting promoterassociated regulatory hypotheses from sequence models and generate a cell-type-resolved map of candidate cis-regulatory elements.